Zhu Keyu, Li Miaomiao, Wu Haibin, Zhang Deyun, Dong Lingli, Wu Qiuhong, Chen Yongxing, Xie Jingzhong, Lu Ping, Guo Guanghao, Zhang Huaizhi, Zhang Panpan, Li Beibei, Li Wenling, Dong Lei, Wang Qifei, Zhu Jinghuan, Hu Wenli, Guo Liqiao, Wang Rongge, Yuan Chengguo, Li Hongjie, Liu Zhiyong, Hua Wei
State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, The Innovative Academy of Seed Design, Chinese Academy of Sciences, Beijing, 100101, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Theor Appl Genet. 2022 Apr;135(4):1235-1245. doi: 10.1007/s00122-021-04027-2. Epub 2022 Jan 10.
Powdery mildew resistance gene MlWE74, originated from wild emmer wheat accession G-748-M, was mapped in an NBS-LRR gene cluster of chromosome 2BS. Wheat powdery mildew, caused by Blumeria graminis f. sp. tritici (Bgt), is a globally devastating disease. Wild emmer wheat (Triticum turgidum var. dicoccoides) is a valuable genetic resource for improving disease resistance in common wheat. A powdery mildew resistance gene was transferred to hexaploid wheat line WE74 from wild emmer accession G-748-M. Genetic analysis revealed that the powdery mildew resistance in WE74 is controlled by a single dominant gene, herein temporarily designated MlWE74. Bulked segregant analysis (BSA) and molecular mapping delimited MlWE74 to the terminal region of chromosome 2BS flanking by markers WGGBD412 and WGGBH346 within a genetic interval of 0.25 cM and corresponding to 799.9 kb genomic region in the Zavitan reference sequence. Sequence annotation revealed two phosphoglycerate mutase-like genes, an alpha/beta-hydrolases gene, and five NBS-LRR disease resistance genes that could serve as candidates for map-based cloning of MlWE74. The geographical location analysis indicated that MlWE74 is mainly distributed in Rosh Pinna and Amirim regions, in the northern part of Israel, where environmental conditions are favorable to the occurrence of powdery mildew. Moreover, the co-segregated marker WGGBD425 is helpful in marker-assisted transfer of MlWE74 into elite cultivars.
抗白粉病基因MlWE74源自野生二粒小麦材料G-748-M,被定位在2BS染色体的一个NBS-LRR基因簇中。由小麦白粉病菌(Blumeria graminis f. sp. tritici,Bgt)引起的小麦白粉病是一种全球性的毁灭性病害。野生二粒小麦(Triticum turgidum var. dicoccoides)是改良普通小麦抗病性的宝贵遗传资源。一个抗白粉病基因从野生二粒小麦材料G-748-M转移到了六倍体小麦品系WE74中。遗传分析表明,WE74中的抗白粉病性由一个单显性基因控制,在此暂时命名为MlWE74。混合分组分析法(BSA)和分子定位将MlWE74定位到2BS染色体的末端区域,两侧标记为WGGBD412和WGGBH346,遗传区间为0.25 cM,对应于Zavitan参考序列中的799.9 kb基因组区域。序列注释揭示了两个磷酸甘油酸变位酶样基因、一个α/β水解酶基因和五个NBS-LRR抗病基因,这些基因可作为基于图谱克隆MlWE74的候选基因。地理位置分析表明,MlWE74主要分布在以色列北部的罗什皮纳和阿米林地区,那里的环境条件有利于白粉病的发生。此外,共分离标记WGGBD425有助于将MlWE74通过标记辅助转移到优良品种中。